HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 968748Generated: October 26, 2026
Hydrochloric Acid → Benzenethiol, 2-amino-3,4,6-trifluoro-, hydrochloride
https://huagongshe.com/reaction/968748
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 4,5,7-Trifluoro-2-methylbenzothiazole | HCID 10375600 | — |
| Solvent | Ethylene Glycol | HCID 174 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | Benzenethiol, 2-amino-3,4,6-trifluoro-, hydrochloride | HCID 11390282 | 73% |
Reaction Steps
A solution of 4,5,7-trifluoro-2-methylbenzothiazole (25.0 g, 123 mmol) in ethylene glycol (310 mL, 0.4 M) and 30% aq. NaOH (310 mL, 0.4 M) was degassed using a nitrogen stream then heated to a gentle reflux (125° C.) for 3 h. The solution was cooled to 0° C. and acidified to pH 3-4 using conc. HCl (approx. 200 mL). The solution was extracted with ether (750 mL) and washed with water (200 mL). The organic layer was dried over Na2SO4, filtered and treated with 2,2-di-tert-butyl-4-methylphenol (0.135 g, 0.5 mol %). After concentrating to dryness, the crude product was dissolved in anhydrous methanol (200 mL) and treated with an HCl solution in 1,4-dioxane (37 mL, 4 N, 148 mmol). The resulting mixture was concentrated to dryness, triturated with isopropylether (100 mL) and filtered to give 2-amino-3,4,6-trifluorothiophenol hydrochloride (19.3 g, 73%) as a light brown solid that was used without further purification. mp. 121-124 C; Rf 0.43 (30% ethyl acetate in heptane); Anal. Calcd for C6H5ClF3NS: C, 33.42; H, 2.34; N, 6.50; S, 14.87. Found C, 33.45; H, 2.27; N, 6.48; S, 14.96.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07304079B2 |
|---|
| Source dataset | uspto-grants-2007_12 |
|---|
| ORD ID | ord-ed09315b92504021b476706db407390a |
|---|
| Source note | uspto-grants-2007_12 |
|---|